A novel SWCNT-polyoxometalate nanohybrid material as an electrode for electrochemical supercapacitors
A novel nanohybrid material that combines single-walled carbon nanotubes (SWCNTs) with a polyoxometalate (TBA) 5 [PV V 2 Mo VI 10 O 40 ] ( TBA-PV 2 Mo 10 , TBA: [(CH 3 (CH 2 ) 3 ) 4 N] + , tetra- n -butyl ammonium) is investigated for the first time as an electrode material for supercapacitors (SCs)...
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Veröffentlicht in: | Nanoscale 2015-05, Vol.7 (17), p.7934-7941 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A novel nanohybrid material that combines single-walled carbon nanotubes (SWCNTs) with a polyoxometalate (TBA)
5
[PV
V
2
Mo
VI
10
O
40
] (
TBA-PV
2
Mo
10
, TBA: [(CH
3
(CH
2
)
3
)
4
N]
+
, tetra-
n
-butyl ammonium) is investigated for the first time as an electrode material for supercapacitors (SCs) in this study. The
SWCNT-TBA-PV
2
Mo
10
material has been prepared by a simple solution method which electrostatically attaches anionic [PV
2
Mo
10
O
40
]
5−
anions with organic TBA cations on the SWCNTs. The electrochemical performance of SWCNT-TBA-PV
2
Mo
10
electrodes is studied in an acidic aqueous electrolyte (1 M H
2
SO
4
) by galvanostatic charge/discharge and cyclic voltammetry. In this
SWCNT-TBA-PV
2
Mo
10
nanohybrid material,
TBA-PV
2
Mo
10
provides redox activity while benefiting from the high electrical conductivity and high double-layer capacitance of the SWCNTs that improve both energy and power density. An assembled
SWCNT-TBA-PV
2
Mo
10
symmetric SC exhibits a 39% higher specific capacitance as compared to a symmetric SC employing only SWCNTs as electrode materials. Furthermore, the
SWCNT-TBA-PV
2
Mo
10
SC exhibits excellent cycling stability, retaining 95% of its specific capacitance after 6500 cycles.
A novel nanohybrid material that combines SWCNTs with a polyoxometalate (TBA)
5
[PV
2
Mo
10
O
40
] (
TBA-PV
2
Mo
10
, TBA: [(CH
3
(CH
2
)
3
)
4
N]
+
) is investigated for the first time as an electrode material for supercapacitors in this work. |
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ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/c4nr07528e |